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4-Bromo-2,6-Dimethylphenol

    • Product Name 4-Bromo-2,6-Dimethylphenol
    • Alias 4-Bromo-2,6-xylenol
    • Einecs 239-218-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    721355

    Cas Number 1834-20-0
    Molecular Formula C8H9BrO
    Molecular Weight 201.06 g/mol
    Iupac Name 4-bromo-2,6-dimethylphenol
    Appearance White to light yellow crystalline powder
    Melting Point 91-93°C
    Boiling Point Unavailable
    Solubility In Water Slightly soluble
    Density 1.57 g/cm³
    Flash Point 155.5°C
    Smiles CC1=CC(=C(C=C1Br)C)O
    Pubchem Cid 16711

    As an accredited 4-Bromo-2,6-Dimethylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Bromo-2,6-Dimethylphenol, labeled with hazard symbols, CAS number, and supplier details.
    Shipping 4-Bromo-2,6-Dimethylphenol is shipped in tightly sealed containers, protected from light and moisture, and clearly labeled according to hazardous material regulations. Transport is conducted in compliance with local and international guidelines, ensuring safe handling to prevent leakage, contamination, or environmental exposure. Standard documentation accompanies each shipment for traceability and safety.
    Storage 4-Bromo-2,6-Dimethylphenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Avoid moisture and sources of ignition. Clearly label the container, and keep it in a secure location designated for hazardous chemicals. Follow all applicable safety and regulatory guidelines.
    Application of 4-Bromo-2,6-Dimethylphenol

    Applications of 4-Bromo-2,6-Dimethylphenol in Industrial Manufacturing

    As a direct manufacturer of 4-Bromo-2,6-Dimethylphenol, we focus on supplying high-purity raw material for advanced formulations in core industrial sectors. Below, we detail specific application pathways with technical parameters and established standards to guide procurement, QA, and process optimization in end-use production lines.

    1. Pharmaceutical Intermediate Synthesis (Antibacterial Actives)

    Pharmaceutical producers use 4-Bromo-2,6-Dimethylphenol as a critical phenolic intermediate to synthesize advanced antibacterial and antifungal agents, primarily in non-oral dosage forms. This intermediate enters the pathway for drugs targeting dermatological conditions and hospital disinfectant actives, especially where broad-spectrum microbial control is essential. Process chemists integrate it during multi-step aromatic substitution and bromination stages, where control of impurities is tightly monitored under validated batch records. QC labs confirm identity and residual solvents as part of GMP protocols before release to formulation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia 12.0 Section 5.10 (Starting Materials for Synthesis)
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals GMP)
    • ICH Q3A/B (Impurities Guidelines)

    Typical usage ratio

    • 0.5% to 10% of compound mass in multistep reaction chains; usage precisely determined by stoichiometric requirements of final API synthesis route

    Downstream process integration

    • Fed into aromatic substitution or condensation steps, often as a limiting reagent in reaction setups for targeted chlorophenol derivatization
    • Processed under nitrogen and mild base in jacketed glass reactors
    • Strictly monitored for residual halide and organic byproducts by HPLC/GC-MS analysis

    Final product types

    • Topical antimicrobial creams
    • Hospital-grade surface disinfectants
    • Dermatological ointments for fungal infections
    • Non-systemic antiseptic formulations

    2. Fine Chemicals Production (Specialty Dyes & Colorants)

    In the dye industry, 4-Bromo-2,6-Dimethylphenol acts as a speciality building block for manufacturing halogenated phenolic derivatives used in high-stability dyes. Dye chemists leverage its brominated structure to introduce precise color and lightfastness in textile and ink systems. The material undergoes controlled diazotization or coupling reactions, with strict in-process controls to achieve desired chromophoric balance and eliminate unreacted phenol residues.

    Industry compliance standards

    • ISO 9001 (Quality Management for Dye Manufacturing)
    • OEKO-TEX Standard 100 (Textile Human Ecological Safety)
    • REACH Annex XVII (Restriction of Dyes and Substances)
    • ZDHC MRSL (Manufacturing Restricted Substances List for Apparel Supply Chains)

    Typical usage ratio

    • 1.5% to 7% of total dye formulation, depending on target color and stability specifications; ratio adjusted per molecular weight of core azo or triphenylmethane systems

    Downstream process integration

    • Introduced during diazotization or electrophilic aromatic substitution in primary colorant synthesis
    • Reacts under pH-controlled, moderately heated systems with real-time spectrophotometric monitoring
    • Downstream purification by crystallization or column chromatography

    Final product types

    • High-performance textile dyes (polyester, nylon, wool)
    • Industrial inks (UV-curable, solvent, flexo)
    • Special effect colorants for automotive coatings
    • Printing inks for packaging

    3. Biocide and Antimicrobial Formulations (Industrial Preservation)

    Formulators in the biocide sector integrate 4-Bromo-2,6-Dimethylphenol into advanced preservation systems for protecting adhesives, polymer dispersions, and water-based coatings against bacterial and fungal contamination. It serves as a core active in formulations where broad-spectrum efficacy is required, meeting regulatory thresholds for in-can and dry-film protection. Processing teams blend it at the dispersion phase, controlling pH and compatibility with other co-preservatives and thickeners to maximize effectiveness and minimize VOC impact.

    Industry compliance standards

    • BPR (EU Biocidal Products Regulation / Regulation (EU) No 528/2012)
    • US EPA FIFRA (40 CFR Part 158 – Data Requirements for Antimicrobial Pesticides)
    • ASTM E645 (Standard Guide for Microbicide Formulation)
    • ISO 11930 (Microbial Protection Preservative Challenge Testing)

    Typical usage ratio

    • 0.08% to 0.25% w/w, defined by product’s intended preservation period, substrate compatibility, and regulatory concentration limits

    Downstream process integration

    • Introduced into aqueous or latex-based formulations at post-emulsification stage
    • Requires homogenous dispersion with minimal agitation to avoid local over-concentration
    • QC validation for broad-spectrum activity and leach resistance via ASTM E2275/E2871

    Final product types

    • Industrial adhesives with in-can protection
    • Waterborne coatings with antimicrobial film
    • Polymer dispersions for flooring and construction
    • Preserved grouts and sealants for construction sector

    4. Chemical Synthesis of Agrochemical Intermediates (Herbicide & Fungicide Bases)

    Producers in the agrochemical sector use 4-Bromo-2,6-Dimethylphenol to build specialty halophenolic cores in herbicide and fungicide active ingredient synthesis. It is incorporated during the formation of pre-emergent herbicide intermediates and as a starting point for triazole or strobilurin-based fungicide production. Downstream synthesis requires high control over residual halide content and byproduct management to ensure compliance with strict agricultural impurity guidelines.

    Industry compliance standards

    • FAO Specification for Agricultural Pesticides
    • ISO 9001:2015 (Quality Management Systems for Agrochemical Manufacturing)
    • EPA PRIA (Pesticide Registration Improvement Act Guidelines, US)
    • OECD Guidelines for the Testing of Chemicals (Series on Pesticides)

    Typical usage ratio

    • 2% to 6% by mass in core active ingredient synthesis; value tailored to specific structure–activity optimization and crop-specific efficacy testing

    Downstream process integration

    • Charged into the initial halogenation or phenolic coupling step, proceeding to multi-stage purification including phase separation and solvent swap
    • Monitored for byproduct formation by LC/MS and GC
    • Final intermediate certified for active loading and trace impurities before granulation or formulation

    Final product types

    • Pre-emergent herbicides for cereals and broadacre crops
    • Systemic and contact fungicides for fruits and vegetables
    • Seed treatment concentrates
    • Granulated agrochemical blends

    5. Resin and Polymer Modifier in High-Performance Materials

    Producers manufacturing specialty polymer systems incorporate 4-Bromo-2,6-Dimethylphenol as a functional modifier within phenolic or epoxy resins. Its halogen content imparts flame retardancy and dimensional stability, especially in molded airline or electronics-grade parts. The compound is metered during pre-polymerization mixing to balance reactivity, crosslink density, and final thermomechanical properties. Production teams validate dispersion, cure kinetics, and post-cure performance per end-use application requirements.

    Industry compliance standards

    • UL 94 (Flammability of Plastic Materials for Parts in Devices and Appliances)
    • RoHS (Restriction of Hazardous Substances Directive, EU)
    • IEC 60216 (Thermal Endurance Properties of Insulating Materials)
    • ISO 1043-4 (Plastics Flame Retardant Additives)

    Typical usage ratio

    • 0.3% to 2.5% of total resin mass, optimized for target flame retardance and mechanical strength per part application

    Downstream process integration

    • Added pre-polymerization to the resin mixing vessel
    • Blended under vacuum to remove residual solvent and ensure complete wet-out
    • Thermoset cured using standard press or continuous molding protocols

    Final product types

    • UL-rated molded electrical components
    • High-performance printed circuit board laminates
    • Aircraft interior panels
    • Industrial appliance housings

    6. Synthesis of Analytical Reagents and Standards

    Manufacturers of laboratory reagents and QC standards rely on 4-Bromo-2,6-Dimethylphenol as a reference substance and precursor for spectrophotometric and chromatographic calibration. It enables trace organic analysis in environmental, pharmaceutical, and materials science sectors. Chemists prepare analytical standards by precise dissolution in compatible solvents under controlled conditions, with product identity, purity, and homogeneity stringently validated under ISO accredited methods before lot release.

    Industry compliance standards

    • ISO 17034 (General Requirements for Reference Material Producers)
    • ISO/IEC 17025 (Testing and Calibration Laboratories Competence)
    • USP General Chapter <11> (Reference Standards)
    • ISO Guide 35 (Reference Material Characterization and Quality Control)

    Typical usage ratio

    • 0.01% to 0.5% in standard preparation; precise weighting performed gravimetrically per analytical protocol requirements

    Downstream process integration

    • Prepared in certified, low-permeability vials or ampoules with batch-unique QR traceability
    • Homogenization by magnetic stir or ultrasonic bath
    • QC batch certified by HPLC/UV and NMR for purity and concentration

    Final product types

    • Certified reference materials (CRM) for organic analysis
    • Spectrochemical calibration kits
    • Trace-level environmental QC standards
    • Raw material qualification sets for pharma and chemical labs
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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-2,6-Dimethylphenol: A Key Intermediate from the Manufacturer's Perspective

    Product Overview and Identity

    4-Bromo-2,6-Dimethylphenol, known by its chemical structure as C8H9BrO, brings a distinct combination of attributes to specialty chemical manufacturing. As a manufacturer, we approach this product from a hands-on understanding of both its chemical behavior and its practical utility. Over the years, the demand for brominated phenols has evolved, guided by the constant search for quality, reliability in production processes, and performance consistency in the end-use formulas. The compound's unique substitution pattern makes it valuable for chemists and formulators aiming to achieve specific properties in their applications.

    Our batches of 4-Bromo-2,6-Dimethylphenol consistently deliver high purity levels, accommodating the strict expectations of research laboratories and diverse industries. Purity speaks directly to reactivity, by-product minimization, and reproducibility, all of which impact customer outcomes. Purity also determines the efficiency of downstream processes, supporting users who need predictable results every time. With a melting point that signals its readiness for solid-state storage and a molecular design that curbs unnecessary volatilization, the compound keeps its integrity under recommended storage conditions. This experience-led approach to design, synthesis, and quality control means users benefit from material that meets high standards for stability and performance.

    Direct Manufacturer’s Experience in Handling and Production

    As manufacturers, the journey from raw material sourcing to batch release covers much more than checklists and certificates. The process starts with high-quality phenolic feedstock and reliable bromine sources. Our reactors and purification units are calibrated to avoid contamination, as even trace impurities change how intermediates behave in your process. Inconsistent raw material quality or uncontrolled reaction parameters lead to product failure, wasted resources, and frustrated timelines. Every drum or packed sample from our line reflects the many layers of in-process monitoring, crystallization, and drying routines. This is not just compliance; it's a matter of pride.

    Production of 4-Bromo-2,6-Dimethylphenol calls for experience with halogenation techniques that withstand scale-up pressures. We’ve tuned our methodology to handle the exothermic nature of bromination, address safety controls, and prevent unwanted byproduct formation. Cooling and mixing systems must match reaction kinetics, otherwise local overheating impacts yield and color. The solid obtained is subjected to multiple wash and filtration steps, with regular QC checks on appearance, melting point, and bromine assay. The learning curve included periods of troubleshooting crystallization issues and equipment fouling, leading us to choose specific grade filtration aids and controlled drying schedules that preserve particle integrity.

    Applications: Observations from the Field

    Practical use has shown that 4-Bromo-2,6-Dimethylphenol finds its greatest value as an intermediate in pharmaceutical synthesis, antimicrobial preparations, and as a precursor in the formation of more complex organics. Medicinal chemists engage this molecule for its reactive phenolic hydrogen and ortho/para-directing methyl groups. The presence of the bromine atom creates entry points for further substitution reactions, allowing for the incorporation of tailored functional groups. In process routes where downstream halogen removal or transformation is necessary, the robustness of this phenol holds up under a range of basic or acidic conditions.

    Many of our long-term partners use 4-Bromo-2,6-Dimethylphenol to generate key scaffolds in drug molecule development. The methyl groups at the 2 and 6 positions modulate electron density and steric profile, giving the chemist a handle to steer activity in lead compound libraries. In the fine chemicals space, this compound appears in processes where selective functionalization of aromatic rings is necessary, but standard phenols lack the correct reactivity. End-users notice a difference in yield and downstream reaction times when working with our material, stemming from absence of off-spec byproducts or colored residues that can complicate the reaction sequence.

    Distinction from Other Phenolic Compounds

    In our years of production, customers often ask how 4-Bromo-2,6-Dimethylphenol compares with other phenolic intermediates, such as plain 2,6-dimethylphenol or 4-chloro-2,6-dimethylphenol. The answer rests in the reactivity profile shaped by the bromine atom. Bromine’s larger atomic radius and lower bond dissociation energy make nucleophilic aromatic substitution easier compared to the chloro analog, especially in routes involving cross-coupling or further aromatic modification. This distinction gives process engineers a more flexible platform for downstream molecular elaboration.

    Comparing this compound with singularly methylated bromophenols, dual methylation adjacent to the phenol oxygen increases the hydrophobicity and decreases the hydrogen-bond-donor strength. These features influence how the molecule interacts with reagents and solvents, altering the course of many catalytic transformations. From the manufacturer’s vantage, this means handling different viscosity and solubility during work-up, with specific attention given to particle size and cake washing protocols. Routine side-by-side trials in our technical lab have established the improved performance of the brominated, dimethylated scaffold in reactions using palladium or copper catalysts. Faster conversion rates and cleaner isolations convince even seasoned chemists of the advantage.

    Unique Production Challenges and Solutions

    Producing 4-Bromo-2,6-Dimethylphenol on scale is a study in anticipation. Bromination, even with automation, demands vigilance and contingency planning. Uncontrolled addition rates risk local excess heat and result in discolored or tarry byproducts. Calibrated addition of bromine, constant temperature surveillance, and robust mixing prevent hotspot formation. We take samples at multiple stages to monitor bromine uptake and reaction progress using titration and NMR methods, so deviations from the set path get spotted rapidly.

    The solid isolated after quenching bromination presents with different particle sizes depending on parent methylphenol source and water content during workup. Standardizing the crystal habit was a non-trivial step. Filterability and wash efficiency both suffered until we adjusted pH and adopted a cooling protocol before filtration. Routine problems in earlier years included excess foaming during neutralization and uneven drying, both addressed by choosing a better balance between mechanical agitation and airflow rates inside our dryer units. Each of these steps has been validated across multiple campaigns to assure reproducibility in particle size, appearance, and assay.

    Safety and Stewardship Practices Observed

    Working with brominated compounds means not only protecting product quality but also ensuring the safety of plant operators and the wider environment. We have mapped out strict engineering controls, including vapor containment, emergency knock-out systems, and dedicated waste neutralization lines. Our waste streams go through chemical treatment to break down reactive bromine species before they mix with other process effluent. On the operator level, PPE requirements and training adjust as scale, temperature, and operation type change.

    Minimizing risks from dust formation and residual vapors involves practical upgrades such as closed transfer systems and regular maintenance of fume hoods and exhausts. Through regular consultation with environmental safety officers and local regulatory updates, we've aligned our operations with both current best practices and the expectations of customers who ask for assurance on sustainable and responsible manufacturing. Our technical teams use real-time monitoring systems to track emissions and process variables, creating an immediate feedback loop for process adjustments and event mitigation.

    Supporting Customer Processes and Problem-Solving

    Beyond product delivery, the support we offer often centers around helping customers unravel real-world process hiccups. Not every process operates at the same scale, solvent regime, or set of temperatures. A recurring topic is solubility: some end users require dissolution at lower temperatures, especially in cosolvent systems, while others look for better dispersion in non-polar matrices. Our technical services team shares solubility data and application notes collected from in-house test runs and customer feedback. In applications where crystallization or precipitation becomes a hurdle, we advise on cosolvent ratios and seeding protocols, drawing from our own process optimization history.

    Process bottlenecks also often trace back to trace impurities that affect catalyst lifetime or color stability of the final product. Our QC records, available upon request, include analysis for trace halides and byproducts which most users find impactful. For customers scaling up from bench to pilot or production scale, we provide material samples from multiple lots, enabling blend studies and process tuning before locking full-scale supply. Troubleshooting unusual outcomes, such as unexpected side reactions or lower than expected yields, becomes far easier when raw material variability is not an unknown parameter.

    Supply Chain Insights and Logistics

    Ensuring a steady, consistent supply of 4-Bromo-2,6-Dimethylphenol is a core part of our operation. Raw materials like methylphenol derivatives and bromine follow their own complex supply chain paths, at times straining global availabilities during surges in demand or regulatory disruptions. Our direct relationships with upstream suppliers offer resilience against sudden shortfalls, reducing risk for customers managing critical production timelines. We maintain strategic reserves and rapid batch capabilities to cover urgent requests.

    Over the years, our logistics approach has evolved, following feedback from users dealing with tight schedules, international compliance requirements, and material handling specifics. We use sturdy, chemical-resistant packaging that guards against moisture and physical stress. Each shipment includes material safety documentation and full traceability to the batch level, building trust through transparency. If colder climates or airport storage conditions threaten product flow, we've arranged for thermal protective shipping and interim warehousing. Temperature excursions and prolonged storage are frequent topics raised—our labs provide studies on product stability under simulated freight conditions, reporting about real shelf life rather than theoretical projections.

    Current Trends and Shifting Customer Needs

    Rapid innovation in pharmaceuticals, agrochemicals, and specialty materials keeps changing the role of specialty phenols. Advances in green chemistry call for more selective, efficient, and environmentally conscious intermediates at every stage. Our team has invested in research on cleaner bromination routes, including the use of solvent recovery systems, reduced solvent loads, and recyclable process auxiliaries. Many clients look for evidence of life cycle thinking before approving new suppliers. Responding to this shift, we document both resource utilization and emissions for our 4-Bromo-2,6-Dimethylphenol, sharing details about improvements over benchmarks set a decade ago.

    Greater regulatory focus, particularly in regions with evolving chemical safety frameworks, means product traceability and impurity control plays a larger role in user confidence. Providing analytical method support and lot-specific impurity fingerprints helps customers manage their own compliance requirements. More users now conduct risk assessments and require information on even low-level impurities that previously would have gone undocumented. Regulatory adaptation calls for keeping calibration standards, reference materials, and validation records up to date, all tasks we’ve embedded in our manufacturing roadmap.

    Continuous Quality Commitment

    Quality does not happen by policy alone. Our operators perform hands-on checks at every stage, not just relying on instrument readouts. Optical purity, melt behavior, and visual color screening, conducted multiple times through the process, supplement chromatographic and spectroscopic assessments. Any deviation in appearance guides investigation before release. Our investment in high-resolution LC and GC methods allows us to confirm both identity and trace components, feeding that data back into our process control systems. Customers working on sensitive or high-purity applications rarely tolerate lot-to-lot variation, and years of feedback reinforce the value of consistently checking even when results trend well inside specification limits.

    Our technical team keeps analysis logs and continuous improvement notes for every campaign, not just for audit purposes but as a learning base for problem-solving. Patterns in complaint rates, color drift, or performance dropouts inform equipment upgrades, operator retraining, or decisions on raw material supplier retesting. As the product’s use cases evolve, periodic technical exchanges with peer manufacturers and application specialists grant us fresh perspectives for addressing issues before they ripple into user supply chains.

    Real-World Case Stories and Customer Experiences

    Feedback from customers drives most of our adjustments. In one typical instance, a pharmaceutical client reported process disruptions tied to inconsistent melting point and color between lots, which turned out to stem from a subtle change in our drying routine. We rechecked our process mapping and isolated a parameter drift at the dryer load stage, making a lasting fix. In another scenario, a customer’s scale-up batch experienced unexpected catalysis inhibition, eventually traced to a source impurity in the feedstock we had not previously targeted. Retesting, root cause analysis, and supplier remediation followed, closing the loop on traceability and restoring customer confidence. These are not isolated cases—hands-on feedback, when handled openly and quickly, turns into process upgrades visible to all downstream users.

    Less visible but equally important are small improvements—such as optimizing granule size or rechecking assumed solubility limits—to match changes in user blending, extrusion, or formulation systems. Some customers now require predictive stability modeling for product stored over one year, prompting analysis routines that track compound evolution under realistic stress tests. This feedback-driven approach keeps us responsive not only to what the chemical is supposed to do, but also how it fits into the evolving needs and realities of end-user operations.

    Final Thoughts on the Value of Direct Manufacturer Supply

    From the manufacturer’s view, products like 4-Bromo-2,6-Dimethylphenol mean much more than a line in a catalog. Real-world synthesis brings out the quirks and opportunities that shape every kilogram shipped. Every lot carries not only molecular specification but also the accumulation of lessons learned, customer stories, and hands-on process modifications. These factors combine into an assurance that what ends up in your process vessel or laboratory truly matches the promise made on paper.

    For those who rely on specialty brominated phenols, the surest value comes from deep-rooted supply partnerships with manufacturers who see beyond routine fulfillment. Openness, documentation, and endless tweaks turn a chemical commodity into a trusted tool for innovation and production success. The difference in reliability, responsiveness, and process support between direct manufacture and trading channels becomes clearer with each new application or project hurdle. 4-Bromo-2,6-Dimethylphenol stands as an example of how sustained experience, ongoing adaptation, and transparent communication can give users exactly what they need—not simply what the specification requires.